"Ambry Genetics"[submitter] AND "OR51B6"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2486811	NM_001004750.1(OR51B6):c.45C>A (p.Phe15Leu)	OR51B5, OR51B6 (F15L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345291	NM_001004750.1(OR51B6):c.156C>A (p.Asn52Lys)	OR51B5, OR51B6 (N52K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623477	NM_001004750.1(OR51B6):c.167C>T (p.Pro56Leu)	OR51B5, OR51B6 (P56L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235169	NM_001004750.1(OR51B6):c.229C>T (p.Pro77Ser)	OR51B5, OR51B6 (P77S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2403125	NM_001004750.1(OR51B6):c.443C>A (p.Thr148Lys)	OR51B5, OR51B6 (T148K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609938	NM_001004750.1(OR51B6):c.455T>G (p.Leu152Arg)	OR51B5, OR51B6 (L152R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558465	NM_001004750.1(OR51B6):c.472G>T (p.Val158Phe)	OR51B5, OR51B6 (V158F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226351	NM_001004750.1(OR51B6):c.479G>A (p.Arg160His)	OR51B5, OR51B6 (R160H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3205773	NM_001004750.1(OR51B6):c.482T>A (p.Leu161Gln)	OR51B5, OR51B6 (L161Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205774	NM_001004750.1(OR51B6):c.556G>T (p.Ala186Ser)	OR51B5, OR51B6 (A186S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363886	NM_001004750.1(OR51B6):c.610A>G (p.Met204Val)	OR51B5, OR51B6 (M204V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226959	NM_001004750.1(OR51B6):c.663G>C (p.Lys221Asn)	OR51B5, OR51B6 (K221N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404548	NM_001004750.1(OR51B6):c.672G>A (p.Met224Ile)	OR51B5, OR51B6 (M224I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205776	NM_001004750.1(OR51B6):c.695G>T (p.Arg232Met)	OR51B5, OR51B6 (R232M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2376222	NM_001004750.1(OR51B6):c.725A>G (p.His242Arg)	OR51B5, OR51B6 (H242R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2360485	NM_001004750.1(OR51B6):c.725A>C (p.His242Pro)	OR51B5, OR51B6 (H242P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205777	NM_001004750.1(OR51B6):c.845C>A (p.Pro282Gln)	OR51B5, OR51B6 (P282Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519756	NM_001004750.1(OR51B6):c.934G>C (p.Ala312Pro)	OR51B5, OR51B6 (A312P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance